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6-methoxy-3-(4-methoxyphenyl)-3,4-dihydroquinazoline is a complex organic compound belonging to the quinazoline family. It is characterized by a quinazoline ring structure, which is a fused pyrimido[4,5-b]benzazepine ring system. The compound features a 6-methoxy group attached to the quinazoline core, and a 4-methoxyphenyl group connected at the 3-position. The 3,4-dihydro prefix indicates that the compound has two hydrogen atoms added to the quinazoline ring, making it a partially saturated derivative. This specific chemical structure may confer unique biological or chemical properties, potentially useful in pharmaceutical or materials science applications. The compound's synthesis and reactivity can be influenced by the electron-donating methoxy groups, which may affect its interactions with other molecules.

845-23-8

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845-23-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 845-23-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,4 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 845-23:
(5*8)+(4*4)+(3*5)+(2*2)+(1*3)=78
78 % 10 = 8
So 845-23-8 is a valid CAS Registry Number.

845-23-8Downstream Products

845-23-8Relevant academic research and scientific papers

Ru(II)-arene complexes with N-substituted 3,4-dihydroquinazoline ligands and catalytic activity for transfer hydrogenation reaction

Mercan, Deniz,?etinkaya, Engin,?ahin, Ertan

supporting information, p. 74 - 81 (2013/07/19)

In this study, N-coordinated 3,4-dihydroquinazoline ruthenium(II) complexes were synthesized by the cleavage reaction of [RuCl2(p-cymene)] 2 with N-substituted 3,4-dihydroquinazolines. In addition, the X-ray crystal structure of 2,4,6-trimethylbenzyl substituted 3,4-dihydroquinazoline Ru(II) complex (1a) is reported. Furthermore, the resulting piano-stool complexes were evaluated as transfer hydrogenation catalysts for reduction of acetophenone in the presence of 2-propanol and KOH at 82°C. All the complexes showed good to excellent performance after 1 h in the conversion of acetophenone to alcohol and the reaction rate was found to be sensitive to changes on the N-substituent. Additionally, the most active catalyst 1a was used in transfer hydrogenation of different ketones to investigate the effect of substituents on ketones.

A new bis-Troeger's base: Synthesis, spectroscopy, crystal structure and isomerization

Valik, Martin,Matejka, Pavel,Herdtweck, Eberhardt,Kral, Vladimir,Dolensky, Bohumil

, p. 1278 - 1302 (2008/09/16)

A new bis-Troeger's base was prepared from a tetraamine precursor as a mixture of two diastereoisomers. One of the isomers has a chair-like geometry, and the other possesses a boat-like geometry, embodying molecular tweezers. A one-pot preparation of bis-

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